A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6085732



Internal ID21994965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:93501903..93501903hg38UCSC Ensembl
chr12:93895679..93895679hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604436
Samples
Known GenesMRPL42
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6085732
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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